Methods for treating acute and subchronic pain
a technology of acute and subchronic pain and analgesics, applied in the field of opioid-induced analgesia, can solve the problems of ineffective opioid analgesics in certain pain conditions, unpleasant dose limitation side effects, and the morphine and related opioids' analgesic benefits can be accompanied by other undesirable effects, so as to achieve the effect of eliminating acute or subchronic pain
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Treatment with Ibudilast Intraperitoneally Shortly Before Subcutaneous Administration of Morphine or Oxycodone
A. Materials and Methods
[0137]Animals
[0138]Pathogen-free adult male Sprague-Dawley rats (300-375 g; Harlan Labs, Madison, Wis.) were used in all experiments. Rats were housed in temperature (23±3° C.) and light (12 h: 12 h light:dark cycle; lights on at 0700) controlled rooms with standard rodent chow and water available ad libitum. All procedures were approved by the Institutional Animal Care and Use Committee of the University of Colorado at Boulder. Each study represents an n=6 per group.
[0139]Drugs
[0140]Morphine sulfate and oxycodone hydrochloride were purchased from Sigma (St. Louis, Mo., USA). Morphine and oxycodone were administered subcutaneously at 4 mg / kg in a dose volume of 1 ml / kg in sterile injection normal saline. Ibudilast was supplied by Avigen (Alameda, Calif., USA). Ibudilast was administered intraperitoneally at 7.5 mg / kg in a dose volume of 2.5 ml / kg in 3...
experiment 1
B. Ability of Ibudilast to Induce Analgesia Alone
[0145]Following baseline withdrawal latency assessments (−45 min), animals received ibudilast or vehicle and were tested again 10 min later to determine if ibudilast or vehicle had any effect on withdrawal latencies. At this time (time 0), the animals received a subcutaneous saline injection (1 ml / kg) to control for conditions in Experiment 2 (see below). Animals were then tested every 10 minutes for 80 min alternating high and low intensity Hargreaves tests.
[0146]As shown in FIGS. 1A-1D, administering ibudilast (7.5 mg / kg intraperitoneally in a dose volume of 2.5 ml / kg in 35% PEG in injection saline) or vehicle (35% PEG in injection saline) had no significant influence on either tail (FIGS. 1A and 1B) or paw (FIGS. 1C and 1D) withdrawal latencies in either the high intensity (FIGS. 1A and 1C) or low intensity (FIGS. 1B and 1D) Hargreaves test. A subsequent subcutaneous saline injection also produced no significant nociceptive change...
experiment 2
C. Ability of Ibudilast to Potentiate Morphine Analgesia
[0147]Following baseline withdrawal latency assessments (−45 min), animals received ibudilast or vehicle (−30 min) and were tested again at −10 min. At time 0, animals received a subcutaneous morphine injection (4 mg / kg in a dose volume of 1 ml / kg in injection saline) and were tested every 10 minutes for 230 min alternating high and low intensity Hargreaves tests.
[0148]As shown in FIGS. 2A-2D, administering ibudilast (7.5 mg / kg intraperitoneally in a dose volume of 2.5 ml / kg in 35% PEG in injection saline) 30 min prior to administration of morphine significantly enhanced the pain suppressive effects of morphine on tail (FIGS. 2A and 2B) and paw (FIGS. 2C and 2D) withdrawal latencies in high (FIGS. 2A and 2C) and low (FIGS. 2B and 2D) intensity Hargreaves tests. Thus, while having little to no effect on its own in the absence of morphine, the glial activation inhibitor ibudilast, when co-administered with morphine, enhanced the...
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